摘要
背景:含壳聚糖化合物已被证明适合于骨替代,但很少有研究表明壳聚糖作为一种游离药物对骨折的影响。目的探讨游离壳聚糖对骨折愈合的影响。 材料与方法:30只成年雄性Sprague-Dawley大鼠,平均体重205 g(200~210 g),随机分为两组。标准股骨骨折在所有老鼠身上被创造出来。每周两次腹腔注射壳聚糖1mg,对照组给予生理盐水。骨折部位术后1、2、4周与对照组比较,每组5例。观察各组大鼠体重、活动及反应情况。前后放射室术后所有骨折均行PHS及显微CT扫描,参数包括:骨痂体积用Perkins体积公式、BV/TV、BV、皮质骨BMD、皮质厚度、骨折部位皮质数计算。牺牲后,铁断裂将大鼠的Mur解剖,仔细清洗骨折周围的肌肉,以保持骨痂的完整性。切片用苏木精和伊红染色,组织学评价康复,复原. 结果:X线和显微CT检查显示,实验组在第2周和第4周骨折愈合情况优于对照组。组织学评价实验组骨折愈合情况优于对照组。两组骨折愈合无统计学差异(P>0.05)。RST周。 结论:全身注射游离壳聚糖能促进大鼠股骨骨折早期至中期的骨愈合过程。
关键词: 壳聚糖,骨,骨折愈合,骨痂,成骨,骨重塑。
图形摘要
Current Drug Targets
Title:Systemic Delivery of Free Chitosan Accelerates Femur Fracture Healing in Rats
Volume: 19 Issue: 5
关键词: 壳聚糖,骨,骨折愈合,骨痂,成骨,骨重塑。
摘要: Background: Chitosan-containing compounds have been shown to be suitable for bone replacement, but few studies demonstrate the impact of the chitosan as a free drug on the fracture.In this study, we aimed to evaluate possible effects of free chitosan on fracture healing.
Materials and Methods: Thirty adult male Sprague-Dawley rats with a mean body weight of 205 g (range from 200g to 210g) were randomly and equally divided into two groups. Standardized femur fractures were created in all rats. Treatments were administered intraperitoneally twice weekly at 1 mg chitosan per injection and the controls were administered physiological saline. The site of the fracture was compared with the control group at 1, 2 and 4 weeks after surgery (n=5 in each group). The weight, activity and reaction of the rats were observed at all the timepoints. Anterior-posterior radiographs and micro-CT scans of all fractures were taken after surgery, and the parameters included: the volume of callus that was calculated using the Perkins volume formula, BV/TV, BV, BMD of cortical bone, cortical thickness, and cortical number at the fracture sites. After sacrifice, fractured femurs from rats were dissected and carefully cleaned of muscle around the fracture callus to preserve callus integrity. Sections were stained with haematoxylin and eosin for histological evaluation of healing.
Result: Radiological (X-ray and micro-CT) evaluation showed that fracture healing of the experimental group was better than control group at the second week and fourth week. Histological evaluation revealed fracture healing of the experimental group was better than control group at the same time. There was no statistically significant difference in fracture healing between the two groups at the first week.
Conclusion: Systemic delivery of free chitosan can accelerate the bone healing process in rat femur fracture at the early-middle stage.
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Cite this article as:
Systemic Delivery of Free Chitosan Accelerates Femur Fracture Healing in Rats, Current Drug Targets 2018; 19 (5) . https://dx.doi.org/10.2174/1389450115666141010150255
DOI https://dx.doi.org/10.2174/1389450115666141010150255 |
Print ISSN 1389-4501 |
Publisher Name Bentham Science Publisher |
Online ISSN 1873-5592 |
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